A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611621



Internal ID16399030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:82422670..82625797hg38UCSC Ensembl
Innerchr8:83334905..83538032hg19UCSC Ensembl
Innerchr8:83497460..83700587hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38203128
hg19203128
hg18203128
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12214n54
Supporting Variantsnssv1117318
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611621
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer